Elucidation of repeat motifs R1- and R2-related TRIOBP variants in autosomal recessive nonsyndromic hearing loss DFNB28 among indigenous South African individuals.
- DOI
- 10.1002/mgg3.2015
- Published
- 2022 Oct
- Container
- Molecular genetics & genomic medicine
- Publisher
- Not recorded
- Open access
- yes
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BibTeX
@article{allodium:10.1002/mgg3.2015,
title = {Elucidation of repeat motifs R1- and R2-related TRIOBP variants in autosomal recessive nonsyndromic hearing loss DFNB28 among indigenous South African individuals.},
author = {Kabahuma RI and Schubert WD and Labuschagne C and Yan D and Pepper MS and Liu XZ},
year = {2022},
journal = {Molecular genetics \& genomic medicine},
doi = {10.1002/mgg3.2015},
url = {https://doi.org/10.1002/mgg3.2015}
}RIS
TY - JOUR TI - Elucidation of repeat motifs R1- and R2-related TRIOBP variants in autosomal recessive nonsyndromic hearing loss DFNB28 among indigenous South African individuals. AU - Kabahuma RI AU - Schubert WD AU - Labuschagne C AU - Yan D AU - Pepper MS AU - Liu XZ PY - 2022 JO - Molecular genetics & genomic medicine DO - 10.1002/mgg3.2015 UR - https://doi.org/10.1002/mgg3.2015 ER -
APA
RI, K., WD, S., C, L., D, Y., MS, P., & XZ, L. (2022). Elucidation of repeat motifs R1- and R2-related TRIOBP variants in autosomal recessive nonsyndromic hearing loss DFNB28 among indigenous South African individuals.. Molecular genetics & genomic medicine. https://doi.org/10.1002/mgg3.2015
Source records
- pubmed · retrieved 2026-09-27T01:15:35.408Z